Thesis advisor: James P. Morken / This dissertation presents the development of catalytic enantioselective synthesis and selective functionalization of geminal or vicinal borylsilanes and bis(boronates). In the first chapter, a modular approach to the catalytic synthesis of enantioenriched anti-1,2-borylsilanes will be described, which is enabled by the stereospecific 1,2-metallate shift that occurs during Pd-catalyzed conjunctive cross-coupling reaction. In the second chapter, the Cu-catalyzed site-selective cross-coupling of vicinal bis(boronates) to an array of electrophiles is developed to provide a new method to construct complex boron-containing products from terminal alkenes. A dramatic rate acceleration in transmetalation to copper is enabled by the neighboring activating boronate group in the substrate. Mechanistic experiments suggest that the formation of a chelated cyclic ate complex may play a role in facilitating the transmetalation. As a follow-up project, the site-selective cross-coupling of vicinal diborylsilanes is also investigated. A Pt-catalyzed enantioselective hydrosilylation of (Z)-1,2-diborylethylene provides access to a vicinal 1,2-diboryl-1-silylalkane that can be used in catalytic cross-coupling reactions. Depending on the catalyst employed and the electrophile class, the coupling reaction can occur at either the α or β carbon relative to the silane center. In the last chapter, a practical method is developed to prepare a TiO2 supported gold nanoparticle catalyst that facilitates the cis-diboration of terminal alkynes. The resulting products can undergo a practical Cu-catalyzed site-selective cross-coupling with proton or other non-aryl/alkenyl electrophiles to yield α-substituted alkenyl boronates with excellent yield and site-selectivity. / Thesis (PhD) — Boston College, 2024. / Submitted to: Boston College. Graduate School of Arts and Sciences. / Discipline: Chemistry.
Identifer | oai:union.ndltd.org:BOSTON/oai:dlib.bc.edu:bc-ir_109932 |
Date | January 2024 |
Creators | Kong, Ziyin |
Publisher | Boston College |
Source Sets | Boston College |
Language | English |
Detected Language | English |
Type | Text, thesis |
Format | electronic, application/pdf |
Rights | Copyright is held by the author, with all rights reserved, unless otherwise noted. |
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